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GTR Home > Conditions/Phenotypes > Dilated cardiomyopathy 1X

Summary

Any familial isolated dilated cardiomyopathy in which the cause of the disease is a mutation in the FKTN gene. [from MONDO]

Available tests

83 tests are in the database for this condition.

Check Related conditions for additional relevant tests.

Genes See tests for all associated and related genes

  • Also known as: CMD1X, FCMD, LGMD2M, LGMDR13, MDDGA4, MDDGB4, MDDGC4, FKTN
    Summary: fukutin

Clinical features

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